Newly identified syndrome causes obesity, intellectual disability
- Date:
- February 3, 2016
- Source:
- The University of Manchester
- Summary:
- Genetic scientists have discovered a new genetic syndrome of obesity, over-eating, mental and behavioral problems in six families, from across the world. The researchers used zebrafish models to study the consequences of chromosome 6 deletion and showed that the deletion has an effect on specific cells in the hypothalamus that produce a hormone called oxytocin.
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Genetic scientists at The University of Manchester have discovered a new genetic syndrome of obesity, over-eating, mental and behavioural problems in six families, from across the world.
Dr Siddharth Banka, Clinical Senior Lecturer at the Manchester Centre for Genomic Medicine, who led the study, explained: "Our team has identified that this new syndrome is caused by a small deletion on chromosome 6 that affects the function of hypothalamus, a region of the brain that plays a number of important roles in the body."
Working in collaboration with Dr Eric Glasgow of the Georgetown University Medical Center in Washington D.C., the two teams used zebrafish models to study the consequences of chromosome 6 deletion and showed that the deletion has an effect on specific cells in the hypothalamus that produce a hormone called oxytocin.
This could help explain why sufferers are often severely obese, find it difficult to control their appetites and are prone to mood swings and being withdrawn, the researchers say.
The study, published in the latest issue of the American Journal of Human Genetics represents an important step in our understanding of how the hypothalamus and oxytocin control appetite and behaviour, says Dr Banka, who is also a Consultant Clinical Geneticist at Saint Mary's Hospital at Manchester. "This finding demonstrates the power of human genetic study of rare conditions."
Although at an early stage, the researchers hope that the findings will help form part of a picture of how the hypothalamus works and may lead to new treatments in the future.
Story Source:
Materials provided by The University of Manchester. Note: Content may be edited for style and length.
Journal Reference:
- Paul R. Kasher, Katherine E. Schertz, Megan Thomas, Adam Jackson, Silvia Annunziata, María J. Ballesta-Martinez, Philippe M. Campeau, Peter E. Clayton, Jennifer L. Eaton, Tiziana Granata, Encarna Guillén-Navarro, Cristina Hernando, Caroline E. Laverriere, Agne Liedén, Olaya Villa-Marcos, Meriel McEntagart, Ann Nordgren, Chiara Pantaleoni, Céline Pebrel-Richard, Catherine Sarret, Francesca L. Sciacca, Ronnie Wright, Bronwyn Kerr, Eric Glasgow, Siddharth Banka. Small 6q16.1 Deletions Encompassing POU3F2 Cause Susceptibility to Obesity and Variable Developmental Delay with Intellectual Disability. The American Journal of Human Genetics, 2016; 98 (2): 363 DOI: 10.1016/j.ajhg.2015.12.014
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